1-(4′-Bromo[1,1′-biphenyl]-4-yl)-3-phenyl-2-propen-1-one
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![1-(4′-Bromo[1,1′-biphenyl]-4-yl)-3-phenyl-2-propen-1-one structure](https://file.echemi.com/fileManage/upload/canonicalSmiles/20220812/2ae6526ae99045c4a7d30351c38d40c6.png "1-(4′-Bromo[1,1′-biphenyl]-4-yl)-3-phenyl-2-propen-1-one")
1-(4′-Bromo[1,1′-biphenyl]-4-yl)-3-phenyl-2-propen-1-one
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CAS No:
85098-88-0
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Formula:
C21H15BrO
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Chemical Name:
1-(4′-Bromo[1,1′-biphenyl]-4-yl)-3-phenyl-2-propen-1-one
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Synonyms:
2-Propen-1-one,1-(4′-bromo[1,1′-biphenyl]-4-yl)-3-phenyl-;1-(4′-Bromo[1,1′-biphenyl]-4-yl)-3-phenyl-2-propen-1-one;1-(4′-Bromobiphenyl-4-yl)-3-phenylpropenone
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CAS No:
1-(4′-Bromo[1,1′-biphenyl]-4-yl)-3-phenyl-2-propen-1-one Use and Manufacturing
The preparation method is to react cinnamic acid with sulfur chloride to generate cinnamic acid chloride, and then react with 4-bromobiphenyl in the presence of anhydrous aluminum trichloride to generate a product.
1-(4-Bromobiphenyl-4-yl)-3-phenyl-2-propen-1-one is an intermediate of the rodenticide bromadiolone.
Computed Properties
Molecular Weight:363.2
XLogP3:5.4
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:362.03063
Monoisotopic Mass:362.03063
Topological Polar Surface Area:17.1
Heavy Atom Count:23
Complexity:394
Defined Bond Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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1-(4′-Bromo[1,1′-biphenyl]-4-yl)-3-phenyl-2-propen-1-one
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